211685-96-0

Basic information

• Product Name: BCC-36
• Synonyms: 3,6-Bis(N-carbazolyl)-N-phenylcarbazole;9′-Phenyl-9,3′:6′,9′′-ter-9H-carbazole;BCC-36;N-Phenyl-3,6-tricarbazolylcarbazole;6-(9H-carbazol-9-yl)-9-phenyl-9H-3,9'-bicarbazole;9-phenyl-9H-3,6,9-Tricarbazol
• CAS NO: 211685-96-0
• Molecular Formula: C₄₂H₂₇N₃
• Molecular Weight: 573.68388
• EINECS: 200-258-5
• Mol File: 211685-96-0.mol
• Article Data: 6

Chemical Properties

• Melting Point: 281-286°C
• Appearance: /
• Density: 1.26±0.1 g/cm3(Predicted)
• CAS DataBase Reference: BCC-36(CAS DataBase Reference)
• NIST Chemistry Reference: BCC-36(211685-96-0)
• EPA Substance Registry System: BCC-36(211685-96-0)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 211685-96-0(Hazardous Substances Data)

Usage

Description

BCC-36 is a host material that is utilized in the creation of efficient solution-processed blue phosphorescent devices. It plays a crucial role in enhancing the performance of these devices by improving their luminance, efficiency, and overall display quality.

Uses

Used in Phosphorescent Device Industry:
BCC-36 is used as a host material for the development of efficient solution-processed blue phosphorescent devices. It serves as a key component in the device structure, contributing to the overall performance and quality of the device.
Device-1:
In the first device, BCC-36 is used in conjunction with ITO/PEDOT:PSS, FIrpic (10 wt%), TAZ, Cs2CO3, and Al. The device exhibits deep blue color, a low turn-on voltage of 3.9 V, a maximum luminance of 19,200 Cd/m2, and an external quantum efficiency (EQE) of 9.7%.
Device-2:
In the second device, BCC-36 is used with ITO/PEDOT:PSS, FIr6 (10 wt%), TAZ, Cs2CO3, and Al. This device also showcases deep blue color, a slightly higher turn-on voltage of 5.0 V, a maximum luminance of 12,300 Cd/m2, and an EQE of 4.1%.
In both applications, BCC-36 plays a vital role in the performance and efficiency of the blue phosphorescent devices, making it a valuable material in the phosphorescent device industry.

Upstream product

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Relevant articles and documents

Carbazole compound, light-emitting element, light-emitting device, electronic device, and lighting device

A novel carbazole compound is provided which can be used as a host material for a light-emitting substance (substance emitting fluorescence or substance emitting phosphorescence). A light-emitting element with high emission efficiency, and a light-emittin

N-phenyl triscarbazole

The present invention relates to a novel triscarbazole compound having substituent on N-phenyl, which can be represented by Formula (I). wherein R1 is selected from the group consisting of halogen or alkyl or alkoxy group having 1 to 20 carbon atoms wherein one or more hydrogen atom may be replaced by halogen; RA, RB, Rc, RD and RE are any of substituents; and i, j, k, l and m are same or different at each occurrence and represent an integer from 0 to 4. By introduction of the substituent on N-phenyl, the device efficiency, stability and lifetime can be increased while maintaining the solubility. These compounds can be used in various organic devices such as organic light emitting diodes, photovoltaic cells or organic semiconductor devices.

Dendritic structure having a potential gradient: New synthesis and properties of carbazole dendrimers

A new synthetic route for carbazole dendrimers was discovered using the copper-catalyzed N-arylation reaction. This synthetic route allowed synthesizing the fourth generation carbazole dendrimer and several derivatives for the first time. The crystal structure, Mark-Houwink-Sakurada plots, and UV-vis and fluorescence studies showed that the dendritic carbazole backbone has a rigid and highly twisted structure. From the measurement of the redox potential of the ferrocene derivatives, the IR spectra of the benzophenone derivatives, and complexation behavior of the phenylazomethine derivatives, the inductive electron-withdrawing effect of the carbazole dendron was revealed. This suggested that the summation of this electron withdrawal from each layer may produce a potential gradient such that the outer layer is electron-rich and the inner layer is electron-poor in the carbazole dendron. By assignment of the 1H and 13C NMR spectra of the dendron, the existence of this kind ofpotential gradient was proved. Overall, these data show the ?-polari zation substituent effect of the carbazole unit, and their summation determines the potential gradient in the repeating dendritic structure of the carbazole dendrimer.